Nitrous Oxide
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Nitrous Oxide
- Generic name
- NITROUS OXIDE
- Manufacturer
- Helget Gas Products
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c8ea7d9d-d0c3-4ce4-a6e0-3ca0286d9795
- SPL ID
- 436c1132-5ac7-b396-e063-6394a90adec4
- Version
- 9
- Effective date
- 2025-11-12
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:45:08
| Harmonized routes |
|---|
| RESPIRATORY (INHALATION) |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | NDA | 206014 | derived:openfda.application_number |
| application number | NDA206014 | openfda.application_number | |
| brand name | Nitrous Oxide | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | Helget Gas Products | openfda.manufacturer_name | |
| ndc | package | 52086-015-06 | openfda.package_ndc |
| ndc | package | 52086-015-05 | openfda.package_ndc |
| ndc | package | 52086-015-04 | openfda.package_ndc |
| ndc | package | 52086-015-01 | openfda.package_ndc |
| ndc | package | 52086-015-03 | openfda.package_ndc |
| ndc | package | 52086-015-02 | openfda.package_ndc |
| ndc | product | 52086-015 | openfda.product_ndc |
| ndc11 | package | 52086001503 | derived:openfda.package_ndc |
| ndc11 | package | 52086001502 | derived:openfda.package_ndc |
| ndc11 | package | 52086001501 | derived:openfda.package_ndc |
| ndc11 | package | 52086001504 | derived:openfda.package_ndc |
| ndc11 | package | 52086001506 | derived:openfda.package_ndc |
| ndc11 | package | 52086001505 | derived:openfda.package_ndc |
| rxcui | 347046 | openfda.rxcui | |
| spl id | 436c1132-5ac7-b396-e063-6394a90adec4 | id | |
| spl set id | c8ea7d9d-d0c3-4ce4-a6e0-3ca0286d9795 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.